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24 Oct 2017, 6:18 am by Rachael G. Pontikes
Chicago Partner Rachael Pontikes of Reed Smith’s Life Science Health Industry group will speak at the Food and Drug Law Institute’s (FDLI) Drug Quality Security Act Conference on November 15 in Washington D.C. [read post]
10 Nov 2015, 1:45 pm by J. Bradley Smith, Esq.
For instance, in North Carolina, the law says that anyone who committed a felony drug crime in another state after 1996 is totally barred from receiving food stamps. [read post]
4 Jan 2019, 5:15 am by CSSFIRM.COM
Contrary to a rule suggested by the Food and Drug Administration (FDA) in 2013 that would have allowed injured The post FDA Decision Allows Generic Drug Makers to Dodge Product Liability Lawsuits appeared first on Childers, Schlueter & Smith, LLC. [read post]
19 Sep 2011, 2:38 am by Cal Warriner
On Thursday, September 15, 2011, the Food and Drug Administration announced that Glaxo Smith Kline’s (GSK) anti-nausea drug Zofran (Ondansetron) has been linked to potentially fatal cardiac arrhythmias. [read post]
2 Jun 2011, 1:41 pm by Lisa Baird
Hamburg (Commissioner of Food and Drugs, US Food and Drug Administration), Wu Zhen (Deputy Commissioner of China's State Food and Drug Administration), Ralph Tyler (Chief Counsel, US Food and Drug Administration), Rosemary Gallant (Principal Commercial Officer Beijing, US Embassy Beijing, Commercial Section), Ding Jianhua (Deputy Director-General, Department of International Cooperation, SFDA), Wang Lanming… [read post]
The United States Food and Drug Administration (FDA) has proposed a rule on “Drug Products or Categories of Drug Products that Present Demonstrable Difficulties for Compounding Under sections 503A or 503B of the Federal Food, Drug, and Cosmetic Act”. [read post]
19 Jun 2017, 1:35 pm by Edward Smith
Cancer Drug Keytruda Is Providing New Hope to Many Hi, I’m Ed Smith, a Sacramento personal injury lawyer. [read post]
19 Oct 2009, 2:07 pm
Food and Drug Administration, White Oak, MD Panel II Caroline Smith DeWaal, Director of Food Policy, Center for Science in the Public Interest, Washington, DC - Testimony Michael Roberson, Food Marketing Institute, Arlington, VA - Testimony Daniel L. [read post]
30 Jul 2012, 12:49 pm by Cal Warriner
So when Smith & Nephew applied to have its Birmingham Hip Resurfacing System (BHR), metal-on-metal (MoM) hip implant approved by the Food and Drug Administration, Wright tried to block the approval. [read post]
Food and Drug Administration (“FDA”) regarding its commitments set forth under the Prescription Drug Under Fee Act Reauthorization Performance Goals and Clinical Trial Diversity and Modernization mandates established by Congress under the Food and Drug Omnibus Reform Act of 2022 (FDORA), including developments on the intersection and use of digital health technology in clinical trials and clinical trial diversity. [read post]
3 Aug 2006, 1:40 pm
In December of 2005 the Food and Drug Administration, along with the makers of Paxil, Glaxo Smith Kline, issued an alert advising of the possible risk of birth defects in pregnant women who use Paxil. [read post]
8 Dec 2015, 11:35 am by J. Bradley Smith, Esq.
feature=watch     See Our Related Blog Posts: Use of criminal law to address societal problems leads to over-criminalization Drug Crimes, Ex-Cons and Food Stamps   [read post]
1 Jul 2018, 8:16 am by Steven D. Schwinn
Upsher-Smith Labs, Inc., that the Federal Food, Drug, and Cosmetic Act preempted a plaintiff's state failure-to-warn claims against a generic drug manufacturer for failure... [read post]
19 Jun 2021, 3:37 pm by Thomas Berg and Douglas Laycock
The interest underlying drug laws may be generally compelling, but not, the court found, as applied to limited use of a drug in worship services. [read post]
1 Sep 2020, 3:41 pm by CSSFIRM.COM
Food and Drug Administration (FDA) of the presence of a The post Zantac Recalled Due to Risk of Cancer Contamination appeared first on Childers, Schlueter & Smith, LLC. [read post]
30 Jul 2019, 10:50 am by CSSFIRM.COM
Food and Drug Administration (FDA) approved new warnings of an increased chance of The post FDA Issues Warnings Regarding Xeljanz (tofacitinib) appeared first on Childers, Schlueter & Smith, LLC. [read post]
27 May 2020, 3:13 pm by CSSFIRM.COM
Food and Drug Administration (FDA) limited the use of Uloric in February of 2019, allopurinol The post Allopurinol Now Primary Medication for Gout appeared first on Childers, Schlueter & Smith, LLC. [read post]
13 May 2021, 7:00 am by CSSFIRM.COM
Food and Drug Administration (FDA) of the presence of a The post Zantac Recalled Due to Risk of Cancer Contamination appeared first on Childers, Schlueter & Smith, LLC. [read post]
28 Nov 2011, 9:43 am by Matthew Huisman
Previously, Kupchyk was an assistant general counsel for litigation at the Food and Drug Administration, according to a Nixon Peabody press release. [read post]